Lysosomal Regulation of mTORC1 by Amino Acids in Mammalian Cells

被引:52
作者
Yao, Yao [1 ]
Jones, Edith [1 ,2 ]
Inoki, Ken [1 ,2 ,3 ]
机构
[1] Univ Michigan, Inst Life Sci, 210 Washtenaw Ave, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Mol & Integrat Physiol, 1137 East Catherine St, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Internal Med, Sch Med, 1500 East Med Enter Dr, Ann Arbor, MI 48109 USA
关键词
mTOR; mTORC1; rapamycin; Rheb; Rag; TSC; lysosome; amino acid; growth factor; HOGG-DUBE-SYNDROME; ACTIVATING PROTEIN COMPLEX; TRANSFER-RNA SYNTHETASE; SMALL GTPASE-RHEB; TUMOR-SUPPRESSOR; RAG GTPASES; GENE-PRODUCT; KINASE ACTIVATION; STRUCTURAL BASIS; BINDING PARTNER;
D O I
10.3390/biom7030051
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mechanistic target of rapamycin complex 1 (mTORC1) is a master regulator of cell growth in eukaryotic cells. The active mTORC1 promotes cellular anabolic processes including protein, pyrimidine, and lipid biosynthesis, and inhibits catabolic processes such as autophagy. Consistent with its growth-promoting functions, hyper-activation of mTORC1 signaling is one of the important pathomechanisms underlying major human health problems including diabetes, neurodegenerative disorders, and cancer. The mTORC1 receives multiple upstream signals such as an abundance of amino acids and growth factors, thus it regulates a wide range of downstream events relevant to cell growth and proliferation control. The regulation of mTORC1 by amino acids is a fast-evolving field with its detailed mechanisms currently being revealed as the precise picture emerges. In this review, we summarize recent progress with respect to biochemical and biological findings in the regulation of mTORC1 signaling on the lysosomal membrane by amino acids.
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页数:18
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